128207002: Giant axonal neuropathy (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Central nervous system finding\Disorder of the central nervous system\Axonal neuropathy\Giant axonal neuropathy
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of nervous system\Giant axonal neuropathy
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Giant axonal neuropathy
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of nervous system\Giant axonal neuropathy
• \Disease\Disorder of body system\Neurological disorder\Neuropathy\Axonal neuropathy\Giant axonal neuropathy
• \Disease\Disorder of body system\Neurological disorder\Hereditary disorder of nervous system\Giant axonal neuropathy
• \Disease\Disorder of body system\Neurological disorder\Disorder of the central nervous system\Axonal neuropathy\Giant axonal neuropathy

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
206449013	Giant axonal neuropathy	en	Synonym	Active	Case insensitive	SNOMED CT core
732172013	Giant axonal neuropathy (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
3777464012	An autosomal recessive condition characterised by progressive degeneration of the central and peripheral nervous system with enlargement of axons.	en	Definition	Active	Case sensitive	SNOMED CT core
3777465013	An autosomal recessive condition characterized by progressive degeneration of the central and peripheral nervous system with enlargement of axons.	en	Definition	Active	Case sensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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